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Last Updated: March 19, 2024

CLINICAL TRIALS PROFILE FOR DALBAVANCIN HYDROCHLORIDE


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All Clinical Trials for dalbavancin hydrochloride

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00057369 ↗ Safety and Efficacy of Dalbavancin Versus Vancomycin in the Treatment of Catheter-Related Bloodstream Infections Unknown status Vicuron Pharmaceuticals Phase 2 2001-02-01 This is a study to evaluate a new medication dosed once a week in the treatment of bacterial infections in the blood from intravenous catheters (CR-BSI). The primary objective is to evaluate the efficacy and safety of dalbavancin in the treatment of adults with CR-BSI relative to a standard of care treatment, vancomycin.
NCT00678106 ↗ Study Of Dalbavancin Drug Levels Achieved In Hospitalized Adolescents Who Are Receiving Antibiotic Therapy For Bacterial Infections Completed Pfizer Phase 1 2008-09-01 Adolescent subjects hospitalized for the treatment of bacterial infections will be given 1 gram of dalbavancin through their veins and levels of dalbavancin in blood and urine will be measured at different time points. Safety labs will also be checked on a regular basis to assess the safety of dalbavancin.
NCT01339091 ↗ Efficacy and Safety of Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure Infections Completed Durata Therapeutics Inc., an affiliate of Allergan plc Phase 3 2011-03-01 The primary object is to compare the early clinical efficacy (after 48-72 hours of therapy) of dalbavancin to the comparator regimen (vancomycin with the option to switch to oral linezolid) for the treatment of patients with a suspected or proven gram-positive bacterial skin or skin structure infection.
NCT01431339 ↗ Efficacy and Safety of Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure Infections Completed Durata Therapeutics Inc., an affiliate of Allergan plc Phase 3 2011-07-01 The primary object is to compare the early clinical efficacy (after 48-72 hours of therapy) of dalbavancin to the comparator regimen (vancomycin with the option to switch to oral linezolid) for the treatment of patients with a suspected or proved gram-positive bacterial skin or skin structure infections.
NCT01946568 ↗ A Single Dose Study To Investigate The Pharmacokinetics and Safety Of Dalbavancin In Hospitalized Children Aged 3 Months to 11 Years. Completed Durata Therapeutics Inc., an affiliate of Allergan plc Phase 1 2013-06-01 A phase one study to characterize the pharmacokinetics of dalbavancin in pediatric patients aged 3 months to 11 years (inclusive) following the intravenous administration of a single dose of dalbavancin.
NCT02127970 ↗ Single Dose vs. Two Dose Regimen of Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure Infections Completed Durata Therapeutics Inc., an affiliate of Allergan plc Phase 3 2014-04-18 To compare the efficacy of treatment with a single dose of dalbavancin 1500 mg to treatment with a two dose regimen of dalbavancin (1000 mg on Day 1 followed by 500 mg on Day 8) in participants with known or suspected Gram-positive acute bacterial skin and skin structure infections (ABSSSI) at 48 -72 hours after initiation of treatment.
NCT02269644 ↗ A P3 Comparator Trial in Community Acquired Bacterial Pneumonia Withdrawn Durata Therapeutics Inc., an affiliate of Allergan plc Phase 3 2015-11-01 This study will be a double-blind, randomized, multicenter trial to assess the safety and efficacy of a single 1500 mg IV dose of dalbavancin plus a single 500 mg IV dose of azithromycin in comparison to an approved antibiotic regimen of linezolid 600 mg every 12 hours for 10-14 days plus a single 500 mg IV dose of azithromycin for the treatment of Community Acquired Bacterial Pneumonia.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for dalbavancin hydrochloride

Condition Name

Condition Name for dalbavancin hydrochloride
Intervention Trials
Bacterial Infections 5
Osteomyelitis 4
Surgical Site Infection 3
Wound Infection 3
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Condition MeSH

Condition MeSH for dalbavancin hydrochloride
Intervention Trials
Infections 16
Infection 15
Communicable Diseases 14
Bacterial Infections 8
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Clinical Trial Locations for dalbavancin hydrochloride

Trials by Country

Trials by Country for dalbavancin hydrochloride
Location Trials
United States 122
South Africa 8
Russian Federation 7
Ukraine 4
Estonia 3
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Trials by US State

Trials by US State for dalbavancin hydrochloride
Location Trials
California 10
Florida 8
North Carolina 7
New York 7
Missouri 6
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Clinical Trial Progress for dalbavancin hydrochloride

Clinical Trial Phase

Clinical Trial Phase for dalbavancin hydrochloride
Clinical Trial Phase Trials
Phase 4 6
Phase 3 7
Phase 2/Phase 3 1
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Clinical Trial Status

Clinical Trial Status for dalbavancin hydrochloride
Clinical Trial Phase Trials
Completed 9
Terminated 5
Not yet recruiting 3
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Clinical Trial Sponsors for dalbavancin hydrochloride

Sponsor Name

Sponsor Name for dalbavancin hydrochloride
Sponsor Trials
Durata Therapeutics Inc., an affiliate of Allergan plc 8
Allergan 8
University of Colorado, Denver 2
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Sponsor Type

Sponsor Type for dalbavancin hydrochloride
Sponsor Trials
Industry 19
Other 15
NIH 1
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